Pharmacia Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pharmacia Diagnostics, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Pharmacia Diagnostics, Inc. has 7 FDA 510(k) cleared medical devices. Based in Columbia, US.
Historical record: 7 cleared submissions from 1990 to 1992. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Pharmacia Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pharmacia Diagnostics, Inc.
7 devices
Cleared
Jul 27, 1992
PHARMACIA CMV IGM ELISA
Microbiology
146d
Cleared
Jul 08, 1992
TOXOPLASMA GONDII (TOXO) IGM ENZYME-LINKED IMMUNO
Microbiology
141d
Cleared
Feb 14, 1992
EBV-VCA IGM ELISA
Microbiology
80d
Cleared
Jan 27, 1992
SERIOLOGICAL TEST KIT/IGM ANTIBODY VARI-ZOST VIRUS
Microbiology
140d
Cleared
Jun 25, 1991
DELFIA(R) 17 -OH-PROGESTERON KIT
Hematology
49d
Cleared
Jul 31, 1990
RUBELLA IGG
Microbiology
35d
Cleared
Jul 24, 1990
TOXOPLASMA GONDII IGG
Microbiology
28d